EP1785134A2 - Thiazol-, Imidazol- und Oxazol-Verbindungen und Behandlung von proteinalterungsbedingten Krankheiten - Google Patents
Thiazol-, Imidazol- und Oxazol-Verbindungen und Behandlung von proteinalterungsbedingten Krankheiten Download PDFInfo
- Publication number
- EP1785134A2 EP1785134A2 EP07003205A EP07003205A EP1785134A2 EP 1785134 A2 EP1785134 A2 EP 1785134A2 EP 07003205 A EP07003205 A EP 07003205A EP 07003205 A EP07003205 A EP 07003205A EP 1785134 A2 EP1785134 A2 EP 1785134A2
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- EP
- European Patent Office
- Prior art keywords
- alkyl
- ring
- substituted
- amino
- nitrogen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 125000000217 alkyl group Chemical group 0.000 claims abstract description 215
- 150000001875 compounds Chemical class 0.000 claims abstract description 174
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- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 112
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 97
- 239000011593 sulfur Chemical group 0.000 claims abstract description 97
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- 239000001301 oxygen Substances 0.000 claims abstract description 83
- 229910052739 hydrogen Chemical group 0.000 claims abstract description 75
- 239000001257 hydrogen Chemical group 0.000 claims abstract description 73
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- NPDLYUOYAGBHFB-WDSKDSINSA-N Asn-Arg Chemical group NC(=O)C[C@H](N)C(=O)N[C@H](C(O)=O)CCCN=C(N)N NPDLYUOYAGBHFB-WDSKDSINSA-N 0.000 claims abstract description 20
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- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical class C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 8
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- ZRKFYGHZFMAOKI-QMGMOQQFSA-N tgfbeta Chemical compound C([C@H](NC(=O)[C@H](C(C)C)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CC(C)C)NC(=O)CNC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CCSC)C(C)C)[C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](C)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N1[C@@H](CCC1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(O)=O)C1=CC=C(O)C=C1 ZRKFYGHZFMAOKI-QMGMOQQFSA-N 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- CBDKQYKMCICBOF-UHFFFAOYSA-N thiazoline Chemical compound C1CN=CS1 CBDKQYKMCICBOF-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 description 1
- 230000001732 thrombotic effect Effects 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- CFOAUYCPAUGDFF-UHFFFAOYSA-N tosmic Chemical compound CC1=CC=C(S(=O)(=O)C[N+]#[C-])C=C1 CFOAUYCPAUGDFF-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 208000001072 type 2 diabetes mellitus Diseases 0.000 description 1
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- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
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Classifications
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- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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Definitions
- the present invention relates to methods for treating certain fibrotic diseases or other indications.
- Glucose and other sugars react with proteins by a non-enzymatic, post-translational modification process called non-enzymatic glycosylation.
- At least a portion of the resulting sugar-derived adducts, called advanced glycosylation end products (AGEs) mature to a molecular species that is very reactive, and can readily bind to amino groups on adjacent proteins, resulting in the formation of AGE cross-links between proteins.
- AGEs advanced glycosylation end products
- Recently a number of classes of compounds have been identified whose members inhibit the formation of the cross-links, or in some cases break the cross-links. These compounds include, for example, the thiazolium compounds described in US Patent No. 5,853,703 .
- AGEs As AGEs, and particularly the resulting cross-links, are linked to several degradations in body function linked with diabetes or age, these compounds have been used, with success, in animal models for such indications. These indications include loss of elasticity in blood vasculature, loss of kidney function and retinopathy.
- VEGF vascular endothelial growth factor
- TGF[beta] vascular endothelial growth factor
- AGE-mediated cross-links agents that inhibit the formation of, or more preferably break, AGE-mediated cross-links. It is not unreasonable to infer that the effects seen are due to the removal of AGE-related molecules that provide a stimulus for the production or release of these growth factors. Removal of such molecules is believed to proceed in part due to the elimination of AGE-related cross-links that lock the AGE-modified proteins in place. Moreover, such compounds also reduce the expression of collagen in conditions associated with excess collagen production. Regardless of the mechanism, now provided are new methods of treating a number of indications.
- the invention relates to a method of treating or ameliorating or preventing an indication of the invention in an animal, including a human, comprising administering an effective amount of a compound of the formula I or IA, wherein the substituent groups are as defined below.
- the compound administered is a compound of formula II, wherein the substituent groups are as defined below.
- a method and compositions are disclosed for, among other things, in an animal, treating the indications described below and (i) improving the elasticity or reducing wrinkles of the skin, treating (ii) diabetes or treating or preventing (iii) adverse sequelae of diabetes, (iv) kidney damage, (v) damage to blood vasculature, (vi) hypertension, (vii) retinopathy, (viii) damage to lens proteins, (ix) cataracts, (x) peripheral neuropathy, or (xi) osteoarthritis.
- the invention further relates to preventing or reversing advanced glycosylation endproducts and cross-linking caused by other reactive sugars present in vivo or in foodstuffs, including ribose, galactose and fructose.
- compositions comprise agents for inhibiting the formation of and reversing the pre-formed advanced glycosylation (glycation) endproducts and breaking the subsequent cross-links. While not wishing to be bound by any theory, it is believed that the breaking of the pre-formed advanced glycosylation (glycation) endproducts and cross-links is a result of the cleavage of alpha-dicarbonyl-based protein crosslinks present in the advanced glycosylation endproducts.
- agents useful in the present invention are members of the class of compounds known as thiazoles, others are imidazoles or oxazoles.
- the compounds, and their compositions, utilized in this invention are believed to react with an early glycosylation product thereby preventing the same from later forming the advanced glycosylation end products that lead to cross-links, and thereby, to molecular or protein aging and other adverse molecular consequences. Additionally, they react with already formed advanced glycosylation end products to reduce the amount of such products.
- compositions containing such proteins would facilitate the extended useful life of the same.
- Presently used food preservatives and discoloration preventatives such as sulfur dioxide, known to cause toxicity including allergy and asthma in animals, can be replaced with compounds such as those described herein.
- the present method has particular therapeutic application as the Maillard process acutely affects several of the significant protein masses in the body, among them collagen, elastin, lens proteins, and the kidney glomerular basement membranes. These proteins deteriorate both with age (hence the application of the term "protein aging") and as a consequence of diabetes. Accordingly, the ability to either retard or substantially inhibit the formation of advanced glycosylation endproducts, and to reduce the amount of cross-links formed between advanced glycosylation endproducts and other proteins in the body carries the promise for treatment of the complications of diabetes and aging for instance, and thereby improving the quality and, perhaps, duration of animal and human life.
- the present agents are also useful in the area of personal appearance and hygiene, as they prevent, and reverse, the staining of teeth by cationic anti-microbial agents with anti-plaque properties, such as chlorhexidine.
- Arteriosclerosis Atherosclerosis, Stiff Vessel Disease, Peripheral Vascular Disease, Coronary Stroke
- Arteriosclerosis is a disease marked by thickening, hardening, and loss of elasticity in arterial walls, of which atherosclerosis is a sub-type. Arteriosclerosis in turn falls within the genus of stiff vessel diseases. Without limitation to theory, it is believed that damage to the blood vessels of these diseases is due to AGE-caused damage, either through protein cross-linking or the stimulation of bioactive agents, or both. Accordingly, the agents are used to treat, prevent, reduce or ameliorate stiff vessel disease, including arteriosclerosis and atherosclerosis. Peripheral vascular disease is an indication that overlaps with atherosclerosis but also covers disease which is believed to have a stronger inflammatory component. First agents are used to treat, prevent, reduce or ameliorate peripheral vascular disease. Coronary heart disease is a form of atherosclerosis of the coronary arteries. First agents are used to treat, prevent, reduce or ameliorate coronary heart disease.
- the ability of the arteries to expand helps to push blood through the body.
- arteries become stiff, as they do in the natural process of aging, the ability of the arteries to expand is diminished and also has consequences for the heart.
- the heart has to work harder to pump the blood into the stiff arteries, and eventually hypertrophies (enlarges in size) to accomplish this.
- a hypertrophied heart is an inefficient pump, and is one of the disorders that leads to congestive heart failure.
- One compound believed to work by a mechanism shared by the compounds of the invention showed an ability to reverse the stiffness of arteries in a Phase IIa clinical trial, as measured by the ratio of stroke volume (ml) to pulse pressure (mm Hg). The potential clinical benefit of this is to lessen the effort that the heart must expend to push blood throughout the body.
- the effect is also believed to contribute to preventing hypertrophy and subsequent inefficiency of the heart, which inefficiency would contribute to congestive heart failure.
- Stroke is a cardiovascular disease that occurs when blood vessels supplying blood (oxygen and nutrients) to the brain burst or are obstructed by a blood clot or other particle. Nerve cells in the affected area of the brain die within minutes of oxygen deprivation and loss of nerve cell function is followed by loss of corresponding bodily function. Of the four main types of stroke, two are caused by blood clots or other particles. These two types are the most common forms of stroke, accounting for about 70-80 percent of all strokes.
- Blood clots usually form in arteries damaged by atherosclerosis. When plaque tears from the sheer forces of blood flowing over an uneven, rigid cap atop the plaque site, thrombotic processes become involved at the "injury" site. As a result, clots can form.
- First agents are used to prevent, reduce or ameliorate the risk of stroke in patients who have suffered previous strokes or have otherwise been identified as at risk.
- First agents can also be used to treat, prevent, reduce or ameliorate peripheral vascular disease and periarticular rigidity.
- Atherosclerosis is a disease that involves deposition of blood lipids in plaque in the arteries throughout the body.
- accumulation of plaque progressively leads to reduced coronary flow, with occlusion of the arteries causing focal death of cardiac tissue (myocardial infarction, heart attack). If the amount of tissue that dies is large enough, death ensues.
- one compound believed to work by a mechanism shared by the compounds of the invention increased the amount of circulating triglycerides (lipids). Consistent with the known presence of AGEs in plaque, the result indicates that the agent had a lipid mobilizing effect on arterial plaque. Reducing local deposits of plaque should eventually lessen the risk of myocardial infarction and death due to heart attacks.
- reducing AGE accumulation at the joints affected by rheumatoid arthritis or osteoarthritis reduces stimulation of the production of cytokines involved in inflammatory processes of the disease.
- Treatment using the invention is expected to treat, prevent, reduce or ameliorate rheumatoid arthritis or osteoarthritis.
- reducing AGE accumulation at bone reduces stimulation of bone resorption.
- the invention is used to treat, prevent, reduce or ameliorate osteoporosis, bone loss or brittle bone.
- agents can be administered as part of a dialysis exchange fluid, thereby preventing, limiting or ameliorating the damage to tissue caused by the sugars found in such exchange fluid.
- agents are expected to prevent, limit or ameliorate the stiffening and sclerosing of peritoneal tissue that occurs in peritoneal dialysis, as well as prevent, limit or ameliorate the formation of new blood vessels in the peritoneal membrane.
- agents are expected to prevent, limit or ameliorate the stiffening and sclerosing of red blood cells and vasculature resulting from exposure to the sugars exchanged into the blood during dialysis.
- Exchange fluids for peritoneal dialysis typically contain 10 - 45 g/L of reducing sugar, typically 25 g/L, which causes the formation of AGEs and consequent stiffening and degradation of peritoneal tissue.
- hemodialysis fluids typically contain up to about 2.7 g/L of reducing sugar, typically 1 to 1.8 g/L.
- the invention provides methods by which the agents are provided in these fluids and thereby prevent, limit or ameliorate the damage that would otherwise result.
- the invention provides methods whereby the agents are administered by the methods described below to prevent, limit or ameliorate such damage from dialysis.
- the exchange fluid preferably contains 0.006 - 2.3 mg/L of an agent of the invention, more preferably, 0.06 to 1.0 mg/L.
- the exchange fluid preferably contains 0.01 to 24 mg/L of an agent of the invention, or preferably, 1.0 to 10 mg/L.
- preventing or ameliorating is effected with a second agent, which is a compound of the aminoguanidine class as described below.
- a preferred route of administration is inclusion in the dialysis fluids.
- the exchange fluid preferably contains 0.125 to 2.5 mg/L of aminoguanidine, more preferably, 0.2 to 1.0 mg/L.
- the exchange fluid preferably contains 1.25 to 25 mg/L of aminoguanidine, or preferably, 2.0 to 10 mg/L.
- the agents are initially administered, and subsequently second agents are used to moderate or limit damage thereafter.
- the agents act to prevent, reduce or ameliorate the restraint on blood flow caused by sickling.
- the mode of action is believed to be in reducing vascular as well as blood cell inelasticity. Accordingly, the agents are used to treat, prevent, reduce or ameliorate sickle cell anemia.
- Diabetic Nephropathy is a complication of diabetes that evolves early, typically before clinical diagnosis of diabetes is made.
- the earliest clinical evidence of nephropathy is the appearance of low but abnormal levels (>30 mg/day or 20 ⁇ g/min) of albumin in the urine (microalbuminuria), followed by albuminuria (>300 mg/24 h or ⁇ 200 ⁇ g/min) that develops over a period of 10-15 years.
- microalbuminuria albuminuria
- albuminuria >300 mg/24 h or ⁇ 200 ⁇ g/min
- GFR glomerular filtration rate
- ESRD End Stage Renal Disease
- the agents are used to treat, prevent, reduce or ameliorate damage to kidney in patients at risk for ESRD.
- the agents can also be used to treat, prevent, reduce or ameliorate glomerulosclerosis.
- Cardiovascular risk correlates more closely with the systolic and the pulse pressure than with the diastolic pressure.
- the cardiovascular risk profile of diabetic patients is strongly correlated to duration of diabetes, glycemic control and blood pressure.
- Structural matrix proteins contribute to the function of vessels and the heart, and changes in the physical behavior of cardiovascular walls are believed to be important determinants of circulatory function.
- the loss of compliance in the aorta leads to isolated systolic hypertension, which in turn expands the arterial wall and thereby diminishes the dynamic range of elasticity.
- canines and in primates indicate potential utility of a compound believed to operate by the AGE-mediated mechanism in substantially ameliorating vascular stiffening.
- the diabetic artery is smaller as it is stiffer.
- First agents are used to treat, prevent, reduce or ameliorate hypertension, including isolated systolic hypertension and diabetic hypertension.
- pulmonary hypertension Pulmonary hypertension is a rare blood vessel disorder of the lung in which the pressure in the pulmonary artery (the blood vessel that leads from the heart to the lungs) rises above normal levels and may become life threatening. The similarity in development of elevated blood pressure in the pulmonary bed with the increase in systemic blood pressure in diabetic hypertension and in isolated systolic hypertension suggests similar mechanisms are involved.
- Pulse pressure is the difference between systolic and diastolic blood pressure.
- systolic pressure In a young human, systolic pressure is typically 120 mm Hg and diastolic pressure is 80 mm Hg, resulting in a pulse pressure of 40 mm Hg.
- pulse pressure With age, in many individuals pulse pressure increases, largely due to the increase in systolic pressure that results from stiff vessel disease. In individuals with pulse pressure greater than 60 mm Hg there is an increased risk of death from cardiovascular morbidities.
- one compound believed to work by a mechanism shared by the compounds of the invention reduced pulse pressure in elderly patients with pulse pressures greater than 60 mm Hg in a statistically significant manner. This decrease in pulse pressure was believed to be due primarily to the effect of the agent on lowering the systolic blood pressure.
- the agents of the invention are used to treat, prevent, reduce or ameliorate reduced vascular compliance, elevated pulse pressure, and hypertension. Moreover, the agents are used to reduce pulse pressure, increase vascular compliance, or decrease the risk of death.
- Congestive Heart Failure is a clinical syndrome that entails cardiac disease of the ventricle.
- Diastolic dysfunction is a subset of heart failure in which the left ventricle stiffens with age. The stiffening of the left ventricle that occurs in CHF and in diastolic dysfunction is believed to result from increased crosslinking of collagen fibers with age and/or fibrosis and related hypertrophy.
- First agents are used to treat, prevent, reduce or ameliorate heart failure.
- diabetic retinopathy The effect of diabetes on the eye is called diabetic retinopathy and involves changes to the circulatory system of the retina.
- the earliest phase of the disease is known as background diabetic retinopathy wherein the arteries in the retina become weakened and leak, forming small, dot-like hemorrhages. These leaking vessels often lead to swelling or edema in the retina and decreased vision.
- the next stage is proliferative diabetic retinopathy, in which circulation problems cause areas of the retina to become oxygen-deprived or ischemic. New vessels develop as the circulatory system attempts to maintain adequate oxygen levels within the retina. Unfortunately, these new vessels hemorrhage easily. In the later phases of the disease, continued abnormal vessel growth and scar tissue may cause serious problems such as retinal detachment and glaucoma.
- First agents are used to treat, prevent, reduce or ameliorate diabetic retinopathy.
- the agents can be administered by the methods described below, including by topical administration to the eye.
- the agents can also be administered by intra
- AGE-mediated crosslinking and/or fibrotic processes are believed to contribute to cataract formation and formation of other damage to lens proteins.
- First agents are used to treat, prevent, reduce or ameliorate cataracts or other damage to lens proteins.
- tau protein neurofibrillary tangles
- beta-amyloid peptide senile plaques
- A.G.E.-modified tau may function as an initiator in a positive feedback loop involving oxidative stress and cytokine gene expression.
- First agents are used to treat, prevent, reduce or ameliorate Alzheimer's disease.
- the invention is believed to be useful in treating, preventing, reducing or ameliorating diabetes or its associated adverse sequelae, and peripheral neuropathy.
- the agents especially in topical form, increase elasticity and/or reduce wrinkles in skin.
- the agents further increase red blood cell deformability.
- agents can be administered concurrently or in a combined formulation with aminoguanidine or other agents of the aminoguanidine class, which are administered in effective amounts as is known in the art. These agents are preferably administered separately from the other compounds described herein. These agents include compounds of formula A wherein R is an alkyl group, or a group of the formula -N(R 4 )(R 5 ) wherein R 4 is hydrogen, and R 5 is an alkyl group or a hydroxyalkyl group; or R 4 and R 5 together with the nitrogen atom are a heterocyclic group containing 4-6 carbon atoms and, in addition to the nitrogen atom, 0-1 oxygen, nitrogen or sulfur atoms; R 1 is hydrogen or an amino group; R 2 is hydrogen or an amino group; R 3 is hydrogen or an alkyl group, wherein R and R 1 cannot both be amino groups.
- R 1 , R 2 , and R 3 is other than hydrogen.
- the compounds can be used as their pharmaceutically acceptable acid addition salts, and mixtures of such compounds.
- aminoguanidine compounds When aminoguanidine compounds are administered, they can be administered by any route of pharmaceutical administration including those discussed below for other first agents.
- the method of the invention is used to treat animals, preferably mammals, preferably humans.
- compositions containing compounds have been developed for the treating the indications of the invention.
- agents are either substituted thiazole, oxazole, or imidazole agents as shown in the Summary section above.
- the invention includes aromatic thiazole, oxazole, and imidazole analogs, as well as non aromatic analogs thereof such as thiazoline, thiazolidine, oxazoline, oxazolidine, imidazoline, and imidazolidine analogs.
- alkyl, and alkenyl groups referred to above include both C1 to C6 linear and branched alkyl and alkenyl groups, unless otherwise noted.
- Alkoxy groups include linear or branched C1 to C6 alkoxy groups, unless otherwise noted.
- Ar refers to a C 6 or C 10 aryl, or a 5 or 6 membered heteroaryl ring.
- the heteroaryl ring contains at least one and up to three atoms of N for the 6 membered heteroaryl ring.
- the 5 membered heteroaryl ring contains; (1) from one to three atoms of N, or (2) one atom of O or S and zero to two atoms of N.
- Nonlimiting examples of heteroaryl groups include: pyrrolyl, furanyl, thienyl, pyridyl, oxazolyl, pyrazolyl, pyrimidinyl, and pyridazinyl.
- Ar can be fused to either a benzene, pyridine, pyrimidine, pyridazine, or (1,2,3) triazine ring.
- C 6 or C 10 aryl groups and heteroaryl containing five or six, or nine to ten ring members are monocyclic or bicyclic.
- the thiazoles, imidazoles, and oxazoles of the invention contain R a and R b substitutions that together with their ring carbons (the C4-C5 carbons of the thiazoles, imidazoles, and oxazoles) form a five to eight membered fused heterocycle (i.e. a bicyclic heterocycle is formed).
- the fused heterocycle is preferably not aromatic.
- Particular compounds within these embodiments contain sulfur atoms in the fused heterocycle (the ring fused to the thiazoles, imidazoles, and oxazoles). These sulfur atoms in these particular compounds can exist in various oxidation states, as S(O) n , where n is 0,1, or 2.
- thiazoles, imidazoles, and oxazoles of the invention contain R a and R b substitutions that together with their ring carbons (the C4-C5 carbons of the thiazoles, imidazoles, and oxazoles) form a C5 to C7 cycloalkyl ring having up to two double bonds including the C4-C5 double bond.
- a cycloalkyl ring is present when R e is a C3 to C8 cycloalkyl ring.
- the cycloalkyl groups can be substituted by one or more of the group consisting of alkyl-, alkoxycarbonyl-, amino-, aminocarbonyl-, carboxy-, fluoro-, or oxo- substituents.
- cycloalkyl groups contain double bonds, the sp 2 hybridized carbon atoms can contain only one substituent (which cannot be amino- or oxo-).
- Sp 3 hybridized carbon atoms in the cycloalkyl ring can be geminally substituted with the exception that (1) two amino groups and (2) one amino and one fluoro group can not be substituted on the same sp 3 hybridized carbon atom.
- the thiazoles, imidazoles, and oxazoles of the invention contain R a and R b substitutions that together with their ring carbons (the C4-C5 carbons of the thiazoles, imidazoles, and oxazoles) form a five or six membered heteroaryl ring (i.e, a bicyclic aromatic heterocycle is formed).
- a preferred bicyclic aromatic heterocycle of the invention is a purine analog [J is N-R d and R a and R b together with their ring carbons (the C4 and C5 of the imidazole ring) form a pyrimidine ring].
- Heterocycles except those of Ar and Ar ⁇ , can be substituted with in addition to any substitutions specifically noted one or more substituents selected from acylamino, alkanoyl, alkoxy, alkoxycarbonyl, alkoxycarbonylalkyl, alkyl, (C1 to C3)alkylenedioxy, alkylamino, alkylsulfonyl, alkylsulfinyl, alkylthio, amino, ArC(O)-, ArO-, Ar-, Ar-alkyl, carboxy, dialkylamino, fluoro, fluoroalkyl, difluoroalkyl, hydroxy, mercapto, oxo, sulfamoyl, trifluoromethyl, 4-[C 6 or C 10 ]arylpiperidin-1-yl and 4-[C 6 or C 10 ]arylpiperazin-1-yl, wherein multiple substituents are located on different atoms of the heterocyclic ring
- halo atoms can be fluoro, chloro, bromo or iodo. Chloro and fluoro are preferred for aryl substitutions.
- such compounds are not
- the method can also comprise administering an amount effective therefor of one or more compounds of formula I , wherein each Ar or cycloalkyl group is substituted with up to two substituents.
- the compounds of formula I, IA and III can form biologically and pharmaceutically acceptable salts.
- Useful salt forms include the halides, particularly the bromide, chloride, tosylate, methanesulfonate, brosylate, fumarate, maleate, succinate, acetate, mesitylenesulfonate and the like.
- Other related salts can be formed using similarly non-toxic, biologically or pharmaceutically acceptable anions.
- R c or R 3 is -NHC(O)(CH 2 ) n -D-R e R f or -NHC(O)(CH 2 ) n -Y- R 5 R 6 are those wherein at least one of R a and R b , or R 1 and R 2 is other than hydrogen.
- the compound is according to Formula I or IA and R c is dialkylamino(C 1 -C 5 )alkyl.
- R c is dialkylamino(C 1 -C 5 )alkyl.
- J is sulfur.
- Useful intermediates include a compound consistent with Formula I or IA, where R c is ⁇ -halo(C 2 -C 5 )alkyl.
- R c is ⁇ -halo(C 2 -C 5 )alkyl.
- J is sulfur.
- the compounds of the invention are capable of inhibiting the formation of advanced glycosylation endproducts on target molecules, including, for instance, proteins, as well as being capable of breaking or reversing already formed advanced glycosylation endproducts on such proteins.
- the cross-linking of protein by formation of advanced glycosylation endproducts contributes to the entrapment of other proteins and results in the development in vivo of conditions such as reduced elasticity and wrinkling of the skin, certain kidney diseases, atherosclerosis, osteoarthritis and the like.
- plant material that undergoes nonenzymatic browning deteriorates and, in the case of foodstuffs, become spoiled or toughened and, consequently, inedible, unpalatable or non-nutritious.
- the compounds employed in accordance with this invention inhibit this late-stage Maillard effect and intervene in the deleterious changes described above, and reduce the level of the advanced glycosylation endproducts already present in the protein material.
- a rationale of the present invention is to use agents which block, as well as reverse, the post-glycosylation step, e.g., the formation of fluorescent chromophores and cross-links, the presence of which is associated with, and leads to adverse sequelae of diabetes and aging.
- An ideal agent would prevent the formation of such chromophores and of cross-links between protein strands and trapping of proteins onto other proteins, such as occurs in arteries and in the kidney, and reverse the level of such cross-link formation already present.
- early glycosylation product(s) as used herein is intended to include any and all such variations within its scope.
- early glycosylation products with carbonyl moieties that are involved in the formation of advanced glycosylation endproducts, and that can be blocked by reaction with the compounds of the present invention have been postulated.
- the early glycosylation product can comprise the reactive carbonyl moieties of Amadori products or their further condensation, dehydration and/or rearrangement products, which can condense to form advanced glycosylation endproducts.
- reactive carbonyl compounds containing one or more carbonyl moieties (such as glycolaldehyde, glyceraldehyde or 3-deoxyglucosone) can form from the cleavage of Amadori or other early glycosylation endproducts, and by subsequent reactions with an amine or Amadori product, can form carbonyl containing advanced glycosylation products such as alkylformyl-glycosylpyrroles.
- carbonyl moieties such as glycolaldehyde, glyceraldehyde or 3-deoxyglucosone
- An AP-dione with the structure of an amino-1,4-dideoxyosone has been isolated by trapping model APs with the AGE-inhibitor aminoguanidine. Subsequent elimination of the 5-hydroxyl gives a 1,4,5-trideoxy-1-alkylamino-2,3-hexulos-4-ene (AP-ene-dione) (3), which has been isolated as a triacetyl derivative of its 1,2-enol form.
- Amadori-diones particularly the AP-ene-dione, would be expected to be highly reactive toward protein crosslinking reactions by serving as targets for the addition of the amine (Lys, His)-, or sulfhydryl (Cys)-based nucleophiles that exist in proteins, thereby producing stable crosslinks of the form (4).
- the linear AP-ene-dione of (3) and the stable cross-link of (4) can cyclize to form either 5- or 6-member lactol rings. See, the scheme shown in US Patent 5,853,703 .
- Therapeutic implications of the present invention relate to the arrest, and to some extent, the reversal of the aging process which has, as indicated earlier, been identified and exemplified in the aging of key proteins by advanced glycosylation and cross-linking.
- body proteins, and particularly structural body proteins, such as collagen, elastin, lens proteins, nerve proteins, kidney glomerular basement membranes and other extravascular matrix components would all benefit in their longevity and operation from the practice of the present invention.
- the present invention thus reduces the incidence of pathologies involving the entrapment of proteins by cross-linked target proteins, such as retinopathy, cataracts, diabetic kidney disease, glomerulosclerosis, peripheral vascular disease, arteriosclerosis obliterans, peripheral neuropathy, stroke, hypertension, atherosclerosis, osteoarthritis, periarticular rigidity, loss of elasticity and wrinkling of skin, stiffening of joints, glomerulonephritis and the like.
- all of these conditions are in evidence and tend to occur at an accelerated rate in patients afflicted with diabetes mellitus as a consequence of this hyperglycemia.
- the present therapeutic method is relevant to treatment of these and related conditions in patients either of advanced age or those suffering from one of the mentioned pathologies.
- Protein cross-linking through advanced glycosylation product formation can decrease solubility of structural proteins such as collagen in vessel walls and can also trap serum proteins, such as lipoproteins to the collagen. Also, this can result in increased permeability of the endothelium and consequently covalent trapping of extravasated plasma proteins in subendothelial matrix, and reduction in susceptibility of both plasma and matrix proteins to physiologic degradation by enzymes. For these reasons, the progressive occlusion of diabetic vessels induced by chronic hyperglycemia is believed to result from excessive formation of glucose-derived cross-links. Such diabetic microvascular changes and microvascular occlusion can be effectively prevented and reversed by chemical inhibition and reversal of the advanced glycosylation product formation utilizing a composition and the methods of the present invention.
- Molecular cross-linking through advanced glycosylation product formation can decrease solubility of structural proteins such as collagen in vessel walls and can also trap serum proteins, such as lipoproteins to the collagen. Also, this can result in increased permeability of the endothelium and consequently covalent trapping of extravasated plasma proteins in subendothelial matrix, and reduction in susceptibility of both plasma and matrix proteins to physiologic degradation by enzymes. For these reasons, the progressive occlusion of diabetic vessels induced by chronic hyperglycemia has been hypothesized to result from excessive formation of sugar-derived and particularly, glucose-derived cross-links. Such diabetic microvascular changes and microvascular occlusion can be effectively prevented and reversed by chemical inhibition and reversal of the advanced glycosylation product formation utilizing a composition and the methods of the present invention.
- diabetes A further consequence of diabetes is the hyperglycemia-induced matrix bone differentiation resulting in decreased bone formation usually associated with chronic diabetes. In animal models, diabetes reduces matrix-induced bone differentiation by 70%.
- compositions of the present invention are utilized for in vivo or therapeutic purposes, it can be noted that the compounds or agents used therein are biocompatible.
- Pharmaceutical compositions can be prepared with a therapeutically effective quantity of the agents or compounds of the present invention and can include a pharmaceutically acceptable carrier, selected from known materials utilized for this purpose. Such compositions can be prepared in a variety of forms, depending on the method of administration. Also, various pharmaceutically acceptable addition salts of the compounds of the invention can be utilized.
- At least one compound of formula I administered in effective amount is not a thiazole substituted on a ring carbon with sulfonamide (the amide of which can be substituted) that has carbonic anhydrase inhibiting activity.
- the composition can include an effective amount of such an agent, as well as a carbonic anhydrase-inhibiting effective amount of another agent, including one of those distinguished above.
- 1-ethylimidazole can be obtained from TCI America (Portland, OR).
- N-(Thiazolidinyl)-4-fluoroaniline N-(Thiazolyl)-2-(4,6-dimethyl-pyrimidin-2-yl-thio)-acetamide, N-(Thiazolyl)-2-(4-propylphenoxy)-acetamide, 2-[4-(N-Furoyl)aminophenyl]-6-methylbenzothiazole, N-(Thiazolyl)-2-(3,5-dimethylphenoxy-acetamide and 2-[(N-(2-Napthalenyl)amino]-[2,3:5,4]-(5,5-dimethyl-cyclohexanonyl)]thiazole can be purchased from MDD, Inc. (Acton, Ontario), a successor to Ortech Corporation.
- a thiazole is reacted with an alkyl or acyl halide in the presence of base such as triethylamine, to produce the corresponding alkyl or acyl derivative at the 2 carbon. See, Medici et al., J. Org. Chem. 49: 590-596, 1984 .
- a chromatographic step is applied to separate additions at the 2 and 3 positions of the thiazole ring.
- 2-Amino thiazole compounds wherein (R c is amino) can also be synthesized by reacting thiourea (which can be substituted on at least one amine) with an alpha-halo ketone using the method described in Vogel's Textbook of Practical Organic Chemistry, 5th Edition, John Wiley & Sons, New York, p. 1153 . Such a reaction is exemplified by a synthesis of 2-amino-4-phenylthiazole:
- Thiazoles substituted on the ring nitrogen can be prepared by alkylation or acylation with appropriate acyl or alkyl halides.
- N-aryl thiazoles and imidazoles can be prepared using appropriate aromatic nucleophilic displacement reactions.
- fluoro phenyl compounds such as 4-fluorobenzoic acid methyl ester can be used to substitute the N 1 nitrogen of imidazole to make methyl-4-(1H-imidazol-1-yl)benzoate. See, Morgan et al., J. Med. Chem. 33: 1091-1097, 1990 .
- Amino functions of 2-aminoimidazoles or 2-aminothiazoles can be acylated by dehydration or other methods known in the art.
- Substituted oxazoles can be prepared by methods known in the art. For instance, 2-unsubstituted oxazoles can be formed by condensation of formamide with either ⁇ -hydroxy or ⁇ -haloketones intermediates ( H. Bredereck, R. Gommper, H. G. v. Shuh and G. Theilig, in Newer Methods of Preparative Organic Chemistry, Vol. III, ed. W. Foerst, Academic press, New York, 1964, p. 241 ). The intermediates can cyclize under acid conditions to form the oxazole ring ( Scheme 2 ). In addition, 2,4-disubstituted oxazoles can be prepared from ⁇ -haloketones and amides at higher temperatures using the same method.
- Oxazoles can be prepared by cyclization reactions of isonitriles ( van Leusen, A. M. Lect. Heterocycl. Chem. 1980, 5, S111 ; Walborsky, H. M.; Periasamy, M. P. in The Chemistry of Functional Groups, suppl. C, Patai, S.; Rappoport, Z., Eds; Wiley-Interscience, 1983, p. 835 ; Hoppe, D. Angew. Chem. Int. Edn. Engl., 1974, 13, 789 ; Schollkopf, U. Angew. Chem. Int. Ed. Engl., 1977, 16, 339 ).
- tosylmethyl isocyanide can be deprotonated by a base and reacted with a suitable electrophile (e.g. an aldehyde).
- a suitable electrophile e.g. an aldehyde
- the intermediate can cyclize and aromatize to provide the desired oxazole analog.
- Other methods for preparing oxazoles include 1,5-dipolar cyclization of acylated nitrile ylides ( Taylor E. C.; Turchi, I. J. Chem. Rev., 1979, 79, 181 ; Huisgen, R. Angew. Chem. Int. Edn. Engl. 1980, 19, 947 )
- 2-Amino-substituted oxazoles can be prepared by two general methods. Urea can be condensed with ⁇ -bromo ketones to yield 2-aminooxazoles that can be substituted at the 4 and 5 positions ( Scheme 4 ). Alternatively, another route to 2-aminooxazoles from acyclic precursors is the base catalyzed reaction of cyanamide with ⁇ -hydroxy ketones ( Scheme 5 ). 2-Aminooxazoles of the invention can also be prepared from the nucleophilic displacement of amines with 2-chlorooxazole, for example, for compounds of the invention wherein R c is ArNH- ( Gompper, R.; Effenberger, F. Chem. Ber., 1959, 92, 1928 ).
- R c is arylcarbonyl
- 2-aminooxazoles can be synthesized by acylation of the amino moiety of 2-aminooxazoles with, for example, with anhydrides to yield 2-acylaminooxazoles.
- 2-aminooxazoles can be acylated, for instance, with chloroacetic anhydride to yield an ⁇ -chloro carboxamide.
- the ⁇ -chloro carboxamide can serve as a suitable alkylating reagent that can be treated with, for example, phenols, arylamines and alkylamines to prepare compounds of the invention.
- An oxazole of the invention wherein Rc is Ar-oxycarbonylamino is shown in Scheme 6 .
- Oxazoles of the invention with Rc is aminocarbonylamino (ureido) or aminothiocarbonylamino (thioureido) can be prepared from 2-aminooxazoles ( Scheme 7 ).
- 2-Aminooxazoles can be treated with isocyanates and isothiocyanates to yield 2-ureido and 2-thioureido oxazoles, respectively ( Crank, G.; Foulis, J. J. Med. Chem., 1971, 14, 1075 : Crank, G. Neville, M.; Ryden, R. J. Med. Chem., 1974, 16, 1402 ).
- 2-Aminooxazoles can be hydrogenated using palladium catalysts to yield 2-aminooxazolines (Scheme 8) ( Tanaka, C.; Kuriyama, S. Yakugaku Zasshi 1979, 99, 78 ).
- Benzoxazole intermediates substituted at the 2 position can be prepared from 2-aminophenols by acylation with, for example, an acid chloride and cyclization ( Scheme 9 ).
- the halomethyl group can be hydrolyzed with, for example, using silver nitrate in water ( Scheme 11 ). Alkylations with amines, including cyclic amines from the same intermediate, are also exemplified.
- R c is hydroxymethyl-, amino (or substituted amino) methyl-, cyclic aminomethyl, or N-imidazol-ylmethyl-
- a 2-hydroxymethyl thiazole can be chlorinated with for example, thionyl chloride, phosphorus pentachloride, or phosphorus oxychloride to give a chloromethyl intermediate that is a suitable for preparing the above mentioned compounds ( Scheme 12 ).
- Methods to prepare the compounds wherein R c is hydroxymethyl and aminomethyl from the chloromethyl intermediate are analogous to those methods illustrated in Scheme 11 .
- R c is hydroxyethyl-, amino(or substituted amino)ethyl-, cyclic aminoethyl, or N-imidazol-ylethyl-
- a 2-hydroxyethyl thiazole intermediate can be prepared from metalation of a thiazole (or by halogen-metal exchange from a 2-bromothiazole) followed by reaction with ethylene oxide.
- the resulting 2-hydroxyethylthiazole can be converted to a chloroethylthiazole using a chlorinating agent, such as thionyl chloride.
- Methods to prepare the compounds wherein R c is hydroxyethyl and aminoethyl from the chloroethyl intermediate are analogous to those methods illustrated in Scheme 11 .
- an effective amount of a pharmaceutical compound will be recognized by clinicians but includes an amount effective to treat, reduce, ameliorate, eliminate or prevent one or more symptoms of the disease sought to be treated or the condition sought to be avoided or treated, or to otherwise produce a clinically recognizable change in the pathology of the disease or condition.
- compositions can be prepared to allow a therapeutically effective quantity of the compound of the present invention, and can include a pharmaceutically acceptable carrier, selected from known materials utilized for this purpose. See, e.g., Remington, The Science and Practice of Pharmacy, 1995 ; Handbook of Pharmaceutical Excipients, 3rd Edition, 1999 . Such compositions can be prepared in a variety of forms, depending on the method of administration.
- compositions of this invention can contain a pharmaceutically-acceptable carrier.
- pharmaceutically-acceptable carrier means one or more compatible solid or liquid filler diluents or encapsulating substances that are suitable for administration to an animal, including a mammal or human.
- compatible means that the components of the composition are capable of being commingled with the subject compound, and with each other, such that there is no interaction that would substantially reduce the pharmaceutical efficacy of the composition under ordinary use.
- the compounds of the invention are soluble in the components of the composition.
- Pharmaceutically-acceptable carriers must, of course, be of sufficiently high purity and sufficiently low toxicity to render them suitable for administration to the animal being treated.
- substances which can serve as pharmaceutically-acceptable carriers or components thereof are sugars, such as lactose, glucose and sucrose; starches, such as corn starch and-potato starch; cellulose and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose, and methyl cellulose; powdered tragacanth; malt; gelatin; talc; solid lubricants, such as stearic acid and magnesium stearate; calcium sulfate; vegetable oils, such as peanut oil, cottonseed oil, sesame oil, olive oil, corn oil and oil of theobroma; polyols such as propylene glycol, glycerine, sorbitol, mannitol, and polyethylene glycol; alginic acid; emulsifiers, such as the Tween TM brand emulsifiers; wetting agents, such sodium lauryl sulfate; coloring agents; flavoring agents; tableting agents, stabilizers; antioxidants;
- a pharmaceutically-acceptable carrier to be used in conjunction with the subject compound is basically determined by the way the compound is to be administered. If the subject compound is to be injected, the preferred pharmaceutically-acceptable carrier is sterile, physiological saline, with a blood-compatible suspending agent, the pH of which has been adjusted to about 7.4.
- the preferred unit dosage form is therefore tablets, capsules, lozenges, chewable tablets, and the like.
- Such unit dosage forms comprise a safe and effective amount of the subject compound, which is preferably from about 0.7 or 3.5 mg to about 280 mg/ 70 kg, more preferably from about 0.5 or 10 mg to about 210 mg/ 70 kg.
- the pharmaceutically-acceptable carrier suitable for the preparation of unit dosage forms for peroral administration are well-known in the art.
- Tablets typically comprise conventional pharmaceutically-compatible adjuvants as inert diluents, such as calcium carbonate, sodium carbonate, mannitol, lactose and cellulose; binders such as starch, gelatin and sucrose; disintegrants such as starch, alginic acid and croscarmelose; lubricants such as magnesium stearate, stearic acid and talc. Glidants such as silicon dioxide can be used to improve flow characteristics of the powder-mixture. Coloring agents, such as the FD&C dyes, can be added for appearance. Sweeteners and flavoring agents, such as aspartame, saccharin, menthol, peppermint, and fruit flavors, are useful adjuvants for chewable tablets.
- inert diluents such as calcium carbonate, sodium carbonate, mannitol, lactose and cellulose
- binders such as starch, gelatin and sucrose
- disintegrants such as starch, alginic acid and cro
- Capsules typically comprise one or more solid diluents disclosed above.
- the selection of carrier components depends on secondary considerations like taste, cost, and shelf stability, which are not critical for the purposes of this invention, and can be readily made by a person skilled in the art.
- Peroral compositions also include liquid solutions, emulsions, suspensions, and the like.
- the pharmaceutically-acceptable carriers suitable for preparation of such compositions are well known in the art.
- Such liquid oral compositions preferably comprise from about 0.012% to about 0.933% of the subject compound, more preferably from about 0.033% to about 0.7%.
- Typical components of carriers for syrups, elixirs, emulsions and suspensions include ethanol, glycerol, propylene glycol, polyethylene glycol, liquid sucrose, sorbitol and water.
- typical suspending agents include methyl cellulose, sodium carboxymethyl cellulose, cellulose (e.g.
- Peroral liquid compositions may also contain one or more components such as sweeteners, flavoring agents and colorants disclosed above.
- compositions useful for attaining systemic delivery of the subject compounds include sublingual and buccal dosage forms.
- Such compositions typically comprise one or more of soluble filler substances such as sucrose, sorbitol and mannitol; and binders such as acacia, microcrystalline cellulose, carboxymethyl cellulose and hydroxypropyl methyl cellulose. Glidants, lubricants, sweeteners, colorants, antioxidants and flavoring agents disclosed above may also be included.
- compositions can also be used to deliver the compound to the site where activity is desired; such as eye drops, gels and creams for ocular disorders.
- compositions of this invention include solutions or emulsions, preferably aqueous solutions or emulsions comprising a safe and effective amount of a subject compound intended for topical intranasal administration.
- Such compositions preferably comprise from about 0.01% to about 10.0% w/v of a subject compound, more preferably from about 0.1% to about 2.0%.
- Similar compositions are preferred for systemic delivery of subject compounds by the intranasal route.
- Compositions intended to deliver the compound systemically by intranasal dosing preferably comprise similar amounts of a subject compound as are determined to be safe and effective by peroral or parenteral administration.
- compositions used for intranasal dosing also typically include safe and effective amounts of preservatives, such as benzalkonium chloride and thimerosal and the like; chelating agents, such as edetate sodium and others; buffers such as phosphate, citrate and acetate; tonicity agents such as sodium chloride, potassium chloride, glycerin, mannitol and others; antioxidants such as ascorbic acid, acetylcystine, sodium metabisulfite and others; aromatic agents; viscosity adjustors, such as polymers, including cellulose and derivatives thereof; and polyvinyl alcohol and acids and bases to adjust the pH of these aqueous compositions as needed.
- the compositions may also comprise local anesthetics or other actives. These compositions can be used as sprays, mists, drops, and the like.
- compositions of this invention include aqueous solutions, suspensions, and dry powders comprising a safe and effective amount of a subject compound intended for atomization and inhalation administration.
- Such compositions are typically contained in a container with attached atomizing means.
- Such compositions also typically include propellants such as chlorofluorocarbons 12/11 and 12/114, and more environmentally friendly fluorocarbons, or other nontoxic volatiles; solvents such as water, glycerol and ethanol, these include cosolvents as needed to solvate or suspend the active; stabilizers such as ascorbic acid, sodium metabisulfite; preservatives such as cetylpyridinium chloride and benzalkonium chloride; tonicity adjustors such as sodium chloride; buffers; and flavoring agents such as sodium saccharin.
- propellants such as chlorofluorocarbons 12/11 and 12/114, and more environmentally friendly fluorocarbons, or other nontoxic volatiles
- solvents such as water, glyce
- compositions of this invention include aqueous solutions comprising a safe and effective amount of a subject compound intended for topical intraocular administration.
- Such compositions preferably comprise from about 0.01% to about 0.8% w/v of a subject compound, more preferably from about 0.05% to about 0.3%.
- compositions also typically include one or more of preservatives, such as benzalkonium chloride or thimerosal; vehicles, such as poloxamers, modified celluloses, povidone and purified water; tonicity adjustors, such as sodium chloride, mannitol and glycerin; buffers such as acetate, citrate, phosphate and borate; antioxidants such as sodium metabisulfite, butylated hydroxy toluene and acetyl cysteine; acids and bases can be used to adjust the pH of these formulations as needed.
- preservatives such as benzalkonium chloride or thimerosal
- vehicles such as poloxamers, modified celluloses, povidone and purified water
- tonicity adjustors such as sodium chloride, mannitol and glycerin
- buffers such as acetate, citrate, phosphate and borate
- antioxidants such as sodium metabisulfite, butylated hydroxy toluen
- compositions of this invention useful for peroral administration include solids, such as tablets and capsules, and liquids, such as solutions, suspensions and emulsions (preferably in soft gelatin capsules), comprising a safe and effective amount of a subject compound.
- Such compositions can be coated by conventional methods, typically with pH or time-dependent coatings, such that the subject compound is released in the gastrointestinal tract at various times to extend the desired action.
- dosage forms typically include, but are not limited to, one or more of cellulose acetate phthalate, polyvinylacetate phthalate, hydroxypropyl methyl cellulose phthalate, ethyl cellulose, Eudragit TM coatings, waxes and shellac.
- the compounds of the invention are administered by ocular, oral, parenteral, including, for example, using formulations suitable as eye drops.
- ointments or droppable liquids may be delivered by ocular delivery systems known to the art such as applicators or eye droppers.
- Such compositions can include mucomimetics such as hyaluronic acid, chondroitin sulfate, hydroxypropyl methylcellulose or polyvinyl alcohol, preservatives such as sorbic acid, EDTA or benzylchromium chloride, and the usual quantities of diluents and/or carriers. See, Remington's Pharmaceutical Sciences, 16th Ed., Mack Publishing, Easton, PA, 1980 , as well as later editions, for information on pharmaceutical compounding.
- the pharmaceutically effective amount is approximately 0.1 or 0.5 to 4 mg/kg body weight daily. Still more preferably, the pharmaceutically effective amount is approximately 1 mg/kg body weight daily. In a preferred embodiment, the amount is administered in once daily doses, each dose being approximately 1 mg/kg body weight.
- the animals then undergo a thoracotomy and the left anterior descending coronary artery iss ligated.
- the chest is then closed and the animals allowed to recover for 14 days while continuing to be treated with compound or placebo.
- the animals are then sacrificed and the hearts removed for histological examination.
- the weight of the infarcted tissue was is measured for the placebo treated animals and compared to the weight for the compound treated animals.
- the thickness of the ventricular wall in the infarcted zone in compound-treated animals is compared to placebo.
- EXAMPLE 1 2,6-diamino-benzothiazole dihydrochloride: 4 g of 2-amino-6-nitrobenzothiazole (Aldrich) was suspended in 130 ml MeOH, and 0.4 g 10% Pd/C (Aldrich) added. The suspension was hydrogenated at room temperature under 60 psi H 2 for 6.5 h. The reaction mixture was filtered, and the particulate washed with MeOH. The filtrate was concentrated under reduced pressure, and crystals formed from the concentrate were collected to yield 2.67 g, mp 196-198°C, yield 81.6%.
- heterocycle includes heteroaryl. Except where heteroaryl is separately recited for the same substituent, the term “heterocycle” includes heteroaryl.
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EP01904934A EP1248615B1 (de) | 2000-01-19 | 2001-01-19 | Thiazol-imidazol- und oxazolverbindungen und behandlung von mit proteinalterung verbundenen erkrankungen |
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EP07003205A Withdrawn EP1785134A3 (de) | 2000-01-19 | 2001-01-19 | Verwendung von Thiazol-, Imidazol- und Oxazol-Verbindungen zur Behandlung von proteinalterungsbedingten Krankheiten |
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Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2312860C2 (ru) | 1999-04-15 | 2007-12-20 | Бристол-Маерс Сквибб Компани | Циклические ингибиторы протеинтирозинкиназ |
EP1359910A4 (de) * | 2000-12-29 | 2006-07-05 | Alteon Inc | Methode zur behandlung von glaukom ii b |
EP1353676A4 (de) * | 2000-12-29 | 2006-05-31 | Alteon Inc | Methode zur behandlung von fibrosen oder anderen indikationen |
JP2006508893A (ja) | 2002-03-15 | 2006-03-16 | イーライ・リリー・アンド・カンパニー | ステロイドホルモン核内レセプターモジュレーターとしてのジヒドロインドール−2−オン誘導体 |
US7049333B2 (en) | 2002-06-04 | 2006-05-23 | Sanofi-Aventis Deutschland Gmbh | Substituted thiophenes: compositions, processes of making, and uses in disease treatment and diagnosis |
DE60323130D1 (de) * | 2002-11-25 | 2008-10-02 | Hoffmann La Roche | Indolderivaten |
US20050137239A1 (en) * | 2003-12-17 | 2005-06-23 | Hines Michelle D. | Thiazole derivatives |
SI3002283T1 (en) | 2003-12-26 | 2018-06-29 | Kyowa Hakko Kirin Co., Ltd. | Thiazole derivatives |
WO2005097766A1 (en) * | 2004-03-31 | 2005-10-20 | Lexicon Genetics, Inc. | 2-aminomethylthiazole-5-carboxamides as protein kinase modulators |
DE602005024274D1 (de) | 2004-07-16 | 2010-12-02 | Sunesis Pharmaceuticals Inc | Als aurora-kinase-inhibitoren nutzbare thienopyrimidine |
WO2006034605A1 (fr) * | 2004-09-28 | 2006-04-06 | Beijing Molecule Science And Technology Co., Ltd. | Nouveaux ammoniums a noyaux azabicycliques et leur utilisation pour le traitement des troubles lies au vieillissement des proteines |
JPWO2006137527A1 (ja) | 2005-06-23 | 2009-01-22 | 協和発酵キリン株式会社 | チアゾール誘導体 |
WO2007070173A2 (en) * | 2005-10-31 | 2007-06-21 | Merck & Co., Inc. | Cetp inhibitors |
CN101007789B (zh) * | 2006-01-27 | 2014-08-20 | 北京摩力克科技有限公司 | 取代五元氮杂环盐类化合物及其治疗蛋白老化相关疾病的用途 |
WO2008050600A1 (fr) * | 2006-10-25 | 2008-05-02 | Neugen Pharma Inc. | Agent thérapeutique ou préventif pour des maladies réfractaires, basé sur la mort cellulaire induite par le stress oxydatif en tant que contexte moléculaire |
CN101668732A (zh) * | 2007-04-02 | 2010-03-10 | 同一世界健康研究院 | Cftr抑制剂化合物及其用途 |
WO2009131951A2 (en) * | 2008-04-21 | 2009-10-29 | Institute For Oneworld Health | Compounds, compositions and methods comprising isoxazole derivatives |
US20100099677A1 (en) * | 2008-04-21 | 2010-04-22 | Institute For Oneworld Health | Compounds, Compositions and Methods Comprising Thiazole Derivatives |
US8207205B2 (en) | 2008-04-21 | 2012-06-26 | Institute For Oneworld Health | Compounds, compositions and methods comprising oxadiazole derivatives |
WO2009131947A2 (en) * | 2008-04-21 | 2009-10-29 | Institute For Oneworld Health | Compounds, compositions and methods comprising pyridazine derivatives |
JP2012503005A (ja) * | 2008-09-19 | 2012-02-02 | インスティテュート フォア ワンワールド ヘルス | イミダゾール誘導体およびトリアゾール誘導体を含む、化合物、組成物ならびに方法。 |
US8343976B2 (en) * | 2009-04-20 | 2013-01-01 | Institute For Oneworld Health | Compounds, compositions and methods comprising pyrazole derivatives |
US20100267706A1 (en) * | 2009-04-20 | 2010-10-21 | Institute For Oneworld Health | Compounds, Compositions and Methods Comprising Pyridazine Derivatives |
CN102942562B (zh) * | 2012-12-05 | 2014-10-01 | 天津市斯芬克司药物研发有限公司 | 一种苯并咪唑衍生物及其制备方法和应用 |
US9622469B2 (en) | 2013-10-03 | 2017-04-18 | David Spiegel | Crosslink breakers for preservation of biological substances |
GB201401886D0 (en) | 2014-02-04 | 2014-03-19 | Lytix Biopharma As | Neurodegenerative therapies |
CZ305633B6 (cs) * | 2014-08-13 | 2016-01-13 | Univerzita Hradec Králové | Deriváty benzothiazolylmočoviny, způsob jejich přípravy a jejich použití |
CN104860937B (zh) * | 2015-04-03 | 2018-02-06 | 北京大学 | 具有β‑分泌酶抑制功能的化合物,制备该化合物的方法及其用途 |
US10344001B2 (en) | 2015-10-02 | 2019-07-09 | Virginia Commonwealth University | Azolylacryloyl derivatives as therapeutic agents for sickle cell disease |
JP2023510431A (ja) * | 2020-01-13 | 2023-03-13 | ザ トラスティーズ オブ コロンビア ユニヴァーシティ イン ザ シティ オブ ニューヨーク | 生体プロテーゼ心臓弁の構造的劣化を軽減させるポリオキサゾリン修飾 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2267089A (en) * | 1992-05-22 | 1993-11-24 | Kotobuki Seiyaku Co Ltd | Cycloheptimidazole derivatives |
US5358960A (en) * | 1984-03-19 | 1994-10-25 | The Rockefeller University | Method for inhibiting advanced glycosylation of proteins using aminosubstituted imidazoles |
WO1996022095A2 (en) * | 1995-01-18 | 1996-07-25 | Alteon Inc. | Use of thiazolium compounds for preventing and reversing the formation of advanced glycosylation endproducts |
WO1997042175A1 (en) * | 1996-05-08 | 1997-11-13 | Alteon Inc. | Substituted imidazolium salts and their use for the inhibition of protein ageing |
WO2002053161A1 (en) * | 2000-12-29 | 2002-07-11 | Alteon, Inc. | Method for treating fibrotic diseases or other indications |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5326779A (en) * | 1984-03-19 | 1994-07-05 | The Rockefeller University | Method of inhibiting the advanced glycosylation of proteins using 1,2-disubstituted-benzimidazoles |
US5258381A (en) * | 1984-03-19 | 1993-11-02 | The Rockefeller University | 2-substituted-2-imidazolines |
WO1992004343A1 (en) * | 1990-09-04 | 1992-03-19 | Yamanouchi Pharmaceutical Co., Ltd. | Novel tetrahydrobenzazole derivative |
FR2677021B1 (fr) * | 1991-05-31 | 1993-10-01 | Upsa Laboratoires | Nouveaux derives de thiazole antagonistes des recepteurs a l'angiotensine ii; leurs procedes de preparation, compositions pharmaceutiques les contenant. |
WO1997006819A1 (en) * | 1995-08-15 | 1997-02-27 | Alteon Inc. | Compositions and methods for elmination of advanced glycosylation endproducts (in vivo) |
US6100282A (en) | 1998-01-02 | 2000-08-08 | Hoffman-La Roche Inc. | Thiazole derivatives |
JP2002503646A (ja) * | 1998-02-13 | 2002-02-05 | ドクトル.ヴイルマル シュヴアベ ゲーエムベーハーウント コンパニー | 安定なハイパーフォリン塩、それらの製造方法、及びそれらのアルツハイマー病の治療のための使用 |
US6265420B1 (en) * | 1998-06-23 | 2001-07-24 | Medinox, Inc. | Use of nitric oxide scavengers to treat side effects caused by therapeutic administration of sources of nitric oxide |
DK1123283T3 (da) | 1998-10-22 | 2004-09-13 | Hoffmann La Roche | Thiazolderivater |
-
2001
- 2001-01-19 EP EP01904934A patent/EP1248615B1/de not_active Expired - Lifetime
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-
2005
- 2005-08-15 US US11/204,231 patent/US20060014781A1/en not_active Abandoned
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5358960A (en) * | 1984-03-19 | 1994-10-25 | The Rockefeller University | Method for inhibiting advanced glycosylation of proteins using aminosubstituted imidazoles |
GB2267089A (en) * | 1992-05-22 | 1993-11-24 | Kotobuki Seiyaku Co Ltd | Cycloheptimidazole derivatives |
WO1996022095A2 (en) * | 1995-01-18 | 1996-07-25 | Alteon Inc. | Use of thiazolium compounds for preventing and reversing the formation of advanced glycosylation endproducts |
WO1997042175A1 (en) * | 1996-05-08 | 1997-11-13 | Alteon Inc. | Substituted imidazolium salts and their use for the inhibition of protein ageing |
WO2002053161A1 (en) * | 2000-12-29 | 2002-07-11 | Alteon, Inc. | Method for treating fibrotic diseases or other indications |
Non-Patent Citations (3)
Title |
---|
DATABASE CA [Online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; DUBOWCHIK, GENE M. ET AL: "Amines That Transport Protons across Bilayer Membranes: Synthesis, Lysosomal Neutralization, and Two-Phase pKa Values by NMR" XP002498311 retrieved from STN Database accession no. 1996:367839 & JOURNAL OF ORGANIC CHEMISTRY, CODEN: JOCEAH; ISSN: 0022-3263, vol. 61, no. 14, 1996, pages 4676-4684, * |
DATABASE CA [Online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; DUBOWCHIK, GENE M. ET AL: "Reversal of doxorubicin resistance and catalytic neutralization of lysosomes by a lipophilic imidazole" XP002498310 retrieved from STN Database accession no. 1994:289617 & BIOCHIMICA ET BIOPHYSICA ACTA, BIOMEMBRANES, CODEN: BBBMBS; ISSN: 0005-2736, vol. 1191, no. 1, 1994, pages 103-108, * |
DATABASE WPI Week 199214 Thomson Scientific, London, GB; AN 1992-114272 XP002498312 & WO 92/04343 A (YAMANOUCHI PHARM CO LTD) 19 March 1992 (1992-03-19) * |
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US20020022622A1 (en) | 2002-02-21 |
KR100766158B1 (ko) | 2007-10-10 |
KR20030016218A (ko) | 2003-02-26 |
DE60128651D1 (de) | 2007-07-12 |
WO2001052847A8 (en) | 2002-09-26 |
EP1248615B1 (de) | 2007-05-30 |
ATE363279T1 (de) | 2007-06-15 |
ES2287096T3 (es) | 2007-12-16 |
MXPA02007099A (es) | 2004-08-23 |
EP1248615A4 (de) | 2004-08-04 |
EP1248615A1 (de) | 2002-10-16 |
CA2397627A1 (en) | 2001-07-26 |
US20060014781A1 (en) | 2006-01-19 |
DE60128651T2 (de) | 2008-01-31 |
US6960605B2 (en) | 2005-11-01 |
CN1426303A (zh) | 2003-06-25 |
AU3286401A (en) | 2001-07-31 |
AU782500B2 (en) | 2005-08-04 |
JP2004501863A (ja) | 2004-01-22 |
EP1785134A3 (de) | 2009-02-18 |
WO2001052847A1 (en) | 2001-07-26 |
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